Letter to the Editor
Ann Lab Med 2021; 41(6): 601-603
Published online November 1, 2021 https://doi.org/10.3343/alm.2021.41.6.601
Copyright © Korean Society for Laboratory Medicine.
Necessity of a Standardized Reporting System of Antiphospholipid Antibody Tests: Relevance for COVID-19
Division of Diagnostic Immunology, Department of Laboratory Medicine, College of Medicine, Hanyang University, Seoul, Korea
Correspondence to: Think-You Kim, M.D.
Division of Diagnostic Immunology, Department of Laboratory Medicine, College of Medicine, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul 04763, Korea
Tel: +82-2-2290-8978, Fax: +82-2-2290-9193
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
We had previously reported that rheumatoid factor is not a contributing factor to the risk of deep vein thrombosis and suggested that autoantibodies such as antiphospholipid antibodies (aPL) could be a possible trigger . In the face of the recent coronavirus disease 2019 (COVID-19) pandemic, among various reports on its clinical features, we have been interested in emerging reports on associations between aPL and thromboembolic events in COVID-19 patients [2–6].
Despite the potential importance of aPL as a clue to the pathogenic mechanism of coagulopathy in COVID-19, these recent reports demonstrate a lack of expertise and no standardized reporting system (Table 1). Therefore, as laboratory physicians, we highlight five key problems associated with reporting aPL test results, with particular relevance to COVID-19.
First, there is a lack of reporting of the antibody titer. Transient elevation of aPL level may occur during infection; therefore, low titers of aPL have low clinical significance. Consequently, reporting the aPL level in numerical form is a very basic and important factor for diagnosing antiphospholipid antibody syndrome (APS), which is based on an anticardiolipin (aCL) level >40 IgG phospholipid (GPL)/IgM phospholipid (MPL) or >99th percentile (p99), or anti-beta-2-glycoprotein I (aβ2GPI) >p99.
Second, there is a lack of reporting of the cut-off value for these tests. The solid-phase aPL test guidelines recommend using the p99 as a cut-off value for both aCL and aβ2GPI tests . However, not all reagents can reflect the p99. In particular, for aCL, GPL or MPL units (U/mL) are still used, and therefore the cut-off for many reagents remains inconsistent with the p99. Some manufacturers provide additional information on the GPL/MPL levels corresponding to the p99; however, 40 GPL/MPL is generally higher than the p99. Considering the variety of cut-off values, the setting condition and related information of the reagents should be carefully checked and presented in reports.
Overall, the p99 is more widely used, especially in new automated systems such as fluorescence enzyme immunoassay (FEIA) and chemiluminescence immunoassay (CLIA) than in conventional ELISA, and in aβ2GPI test reagents than in aCL test reagents. However, in the field of obstetric medicine, the inclusion of low-titer aCL and aβ2GPI for the diagnosis of purely obstetric APS has been continuously recommended; therefore, there are different views on the appropriate cut-off value with respect to the 95th or 97.5th percentile .
Third, the detailed methods and manufacturers of kits are often not mentioned in these reports. Various reagents are used for ELISA worldwide, which show corresponding variability; however, more recent automation systems such as FEIA and CLIA tend to reduce the variability. Moreover, CLIA is characterized by significantly improved background noise, which can be more sensitive than other methods. Therefore, information on the methodology and manufacturers is crucial for establishing a diagnosis of APS.
Fourth, there is a lack of clarity in the reports on IgA aPL. IgA is recommended for interpreting the clinical implications of aPL when both IgG and IgM tests are negative. However, the results of IgA tests are rarely reported, and there is insufficient data and lack of consensus of the clinical relevance. This issue should be handled with caution as a sensitive subject in case reports. Unlike IgG and IgM, IgA measurement cannot be calibrated; Thus, the basic information for the test described above is more essential.
Fifth, the possibility of a false-positive result for the lupus anticoagulant (LA) test is rarely considered. The challenge of securing an adequate sample is a more fundamental issue than standardizing the procedure in actual LA testing. In recent reports, highly frequent LA positivity of 45% (25/56) and 83.3% (5/6) was found in COVID-19 patients without thromboembolism and in stroke patients, respectively [3, 4]. However, the possibility of false positives cannot be excluded due to a high C-reactive protein level or the anticoagulant drug dosed for coagulopathy management [9, 10]. A false-positive LA result is more likely when compared to the positive result frequency of solid-phase aPL tests of only 10% (5/50) and 16.7% (1/6) in these two studies, respectively. Therefore, LA testing in an acute ill state is not recommended .
In closing, the substantial confusion caused by the COVID-19 pandemic can be likened to a Korean proverb: “No matter the urgency, you must thread through the eye of the needle not around the needle.” That is, to obtain reliable results, the basics and principles of laboratory testing and reporting need to be followed and maintained under the current urgency of the pandemic more stringently than ever. In particular, the reporting of titers, cut-offs, test methods, manufacturers, and other detailed information can be used as a basic principle to reduce the confusion regarding inter-assay variability, allowing clinicians to obtain more accurate information on the condition of their patients. Checking for antibody persistence or verification using other methods is also recommended. The LA testing should not be considered in an acute ill state due to sample problem.
Standardization of aPL tests is an ongoing issue, with continuous efforts from various international committees to achieve a consensus. Thus, we hope that COVID-19 would be a trigger to find a resolution.
Kim TY developed the concept for this manuscript. Kim TY and Jearn LH wrote and reviewed the manuscript. Kim TY and Jearn LH read and approved the final manuscript.
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